z-logo
Premium
Iodine‐Mediated Oxidation of Ynamides: A Facile Access to N ‐Monosubstituted α‐Ketoamides and α‐Ketoimides
Author(s) -
Huang Hai,
He Guangke,
Zhu Xiaolin,
Jin Xiaodong,
Qiu Shineng,
Zhu Hongjun
Publication year - 2014
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201402538
Subject(s) - chemistry , iodine , catalysis , functional group , oxidative phosphorylation , reaction conditions , combinatorial chemistry , metal , redox , organic chemistry , medicinal chemistry , biochemistry , polymer
An efficient iodine‐mediated oxidation reaction for ynamides has been developed to produce N ‐monosubstituted α‐ketoamides and α‐ketoimides. This oxidative method, which exhibits good functional group tolerance, was performed under mild conditions without a metal catalyst.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom